Gynecological Symptoms and Health-related Quality of Life in Egyptian Women With SLE

Sponsor
Fayoum University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05230316
Collaborator
(none)
70
2
2.5
35
14

Study Details

Study Description

Brief Summary

The purpose of our study was to Recognize gynecological symptoms and health-related quality of life in Egyptian women with systemic lupus erythematosus and evaluate the impact of duration of remission on QOL in SLE patients.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Despite significant advances in recent decades, systemic lupus erythematosus (SLE) is still burdened by irreversible organ damage and a notable impact on health-related quality of life (HRQoL). Improving the quality of life is a pivotal goal in the management of SLE. According to the Treat to Target (T2T) recommendations for SLE management, particular attention needs to be paid to the factors that negatively influence HRQoL such as fatigue, pain and depression.

    Recent epidemiological studies demonstrate that prolonged remission is an achievable target in SLE patients and is clearly associated with better outcomes in terms of damage accrual. Such findings also raise questions about the possible impact of remission on HRQoL. In a retrospective study, Patients in prolonged remission reported significantly better HRQoL as assessed by the 36-Item Short-Form Health Survey (SF36) and Lupus PRO questionnaire.

    Methodology in details L:

    70 women with SLE will be included in this study from the outpatient clinic. in Fayoum University hospital It will be conducted in the Department of Obstetrics and Gynecology, Fayoum University Maternity Hospital, Egypt.

    Full history taking (Age, Duration of marriage, Parity, Occupation, Mode of delivery, History of abortion, Medical and Surgical history).

    Menstrual histories obtained from participants included: age at menarche, duration of heavy bleeding, duration of menses and menstrual cycle, and other gynecological symptoms as Questionnaire form.

    Patients' blood pressure, height, weight, body mass index (BMI), and other clinical parameters were reviewed by the attending doctors.

    The patient's medications, which included immunosuppressive therapy such as steroids, cyclophosphamide, azathioprine, and cyclosporine A, where noted, and the use of other adjunctive medications were also recorded.

    Definition of remission Definition of remission was in line with European Consensus Criteria . Clinical remission (CLR) was present when clinical SLEDAI score=0 and physician global score less than 0.5

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    70 participants
    Observational Model:
    Cohort
    Time Perspective:
    Cross-Sectional
    Official Title:
    Recognizing Gynecological Symptoms and Health-related Quality of Life in Egyptian Women With Systemic Lupus Erythematosus
    Actual Study Start Date :
    Jan 15, 2022
    Anticipated Primary Completion Date :
    Apr 1, 2022
    Anticipated Study Completion Date :
    Apr 1, 2022

    Outcome Measures

    Primary Outcome Measures

    1. Recognize gynecological symptoms in Egyptian women with systemic lupus erythematosus. [3 month]

      Normal menstrual pattern duration of each menses was between five and 13 days, and the menstrual cycle was between 21 and 35 days. Menarche was defined as the first menstrual period. Oligomenorrhoea was defined as menses occuring at intervals longer than 35 days. Secondary amenorrhoea was defined as the cessation of menses after menstrual cycle has begun and lasted for at least four months for patients with regular cycles, or for at least three of the previous three cycle intervals for patients with irregular cycles.(4) Transient amenorrhoea was defined as when patients resumed her own "normal" cycle after episodes of amenorrhoea, and sustained amenorrhoea was when the patient remained amenorrhoeic until the interview date.

    2. Recognize health related quality of life in Egyptian women with systemic lupus erythematosus. [3 months]

      According to the Treat to Target (T2T) recommendations for SLE management, particular attention needs to be paid to the factors that negatively influence HRQoL such as fatigue, pain and depression.

    Secondary Outcome Measures

    1. Evaluate the impact of duration of remission on QOL in SLE patients. [3 months]

      Clinical remission (CLR) is present when clinical SLEDAI score=0

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    15 Years to 55 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Patients fulfilling the American College of Rheumatology (ACR) 1982 revised criteria for SLE,

    2. age between 15 and 55 years

    3. and consented to the interview.

    Exclusion Criteria:
    1. Patients with active malignancy

    2. and end-stage lupus nephritis

    3. Patients who had been treated with Belimumab in the last 7 years, due to the reported effects of Belimumab on HRQoL.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Fayoum university faculity of medicine Fayoum Fayoum University Zone Egypt 63514
    2 Fayoum university Fayoum Egypt 63514

    Sponsors and Collaborators

    • Fayoum University

    Investigators

    • Study Director: Laila E Abdelfattah, Ass. prof, Associated professor of obestatrics and gynecology Faculty of medicine Fayoume university
    • Principal Investigator: rehab A aboshama, lecturer, lecturer of obstetrics and gynecology

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    rehab abdelhamid aboshama, lecturer of obstetrics and gynecology Faculty of medicine, Fayoum University
    ClinicalTrials.gov Identifier:
    NCT05230316
    Other Study ID Numbers:
    • R 205
    First Posted:
    Feb 8, 2022
    Last Update Posted:
    Apr 12, 2022
    Last Verified:
    Apr 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by rehab abdelhamid aboshama, lecturer of obstetrics and gynecology Faculty of medicine, Fayoum University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 12, 2022